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Screening of key genes and bioinformatics analysis of sepsis-induced myocardial dysfunction#br# |
JIANG Wanwei YANG Guohui |
School of Clinical Medicine, Guizhou Medical University, Guizhou Province, Guiyang 550004, China |
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Abstract Objective To screen the key genes of sepsis-induced myocardial dysfunction (SIMD), and analyze the main biological processes. Methods Data sets of sepsis patients and SIMD mouse models were analyzed differentially by R software, genes related to SIMD were extracted, biological analysis, correlation analysis, and protein-protein interaction network analysis were carried out. Results There were 318 and 143 differential genes in sepsis patients and animal models respectively, including 84 SIMD genes, 54 down-regulated genes and 30 up-regulated genes. Sepsis and SIMD differential genes had similar biological functions in gene ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analysis. ANXA3, S100A8, LCN2, LTF, and KLHL2 were the key genes of SIMD; LTF, LCN2, and SOCS3 were the key proteins of SIMD. Conclusion Many key genes, such as LCN2, LTF, ANXA3, S100A8, KLHL2, and SOCS3 may involve in the pathophysiological process of SIMD, it is significant to further study the clinical diagnosis, prognosis, and treatment of SIMD.
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